The Effect of HIIT in Handling Obesity in Children

NCT ID: NCT03433690

Last Updated: 2018-02-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-07-28

Study Completion Date

2018-01-25

Brief Summary

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In this study the investigators wish to investigate whether a short duration High-intensity Interval Training(HIT) is superior to a moderate activity training modus with regards to improving weight-loss, Blood pressure and sleep quality in severely obese children and adolescents also receiving a multidisciplinary treatment regime.

Detailed Description

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Prevalence of overweight and obesity among children and adolescents are rapidly rising worldwide. Despite the alarming situation, great confusion of how to tackle obesity persists for two main reasons: the condition is much more complex than initially thought, and many aspects regarding pathophysiology remain unrevealed, leading to an insufficient understanding of the disorder. Childhood obesity is, strongly associated with numerous disorders e.g. hypertension, insuline resistance, sleep apnea, depression and many more.

High intensity Interval Training has proven beneficial in treating obesity and comorbidities in adults. The investigators wish to investigate whether twelve weeks of High-intensity Interval Training(HIT) twice a week is superior to a moderate activity training modus for same period of time with regards to improving weight loss, blood pressure and sleep quality, in severely obese children and adolescents also receiving a multidisciplinary treatment regime. Participants are severely obese children and adolescents referred to the outpatient Clinic for treatment of obesity. Participants are randomizid to either moderate training or HIIT. Antropometric measures, blood pressure and sleep quality as measured by sensewear armbands, are done at baseline, after the twelve weeks of training and again one year after inclusion. Participants are monitored with pulse monitors during training sessions to register if training goals are obtained.

Conditions

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High Intensity Interval Training Child Obesity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomized Controlled trial
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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High Intensity Interval Training

Twelve weeks of High Intensity Interval Training, twice a week, in combination with multidisciplinary treatment at outpatient obesity clinic.

Group Type EXPERIMENTAL

HIIT

Intervention Type BEHAVIORAL

High Intensity Interval Training for twelve weeks

Moderate training

Twelve weeks of Moderate Training, twice a week, in combination with multidisciplinary treatment at outpatient obesity clinic.

Group Type ACTIVE_COMPARATOR

Moderate training

Intervention Type BEHAVIORAL

Moderate training for twelve weeks

Interventions

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HIIT

High Intensity Interval Training for twelve weeks

Intervention Type BEHAVIORAL

Moderate training

Moderate training for twelve weeks

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Iso-BMI \> 30 according to the IOTF iso-BMI cut-off points
* Age 8-18 years of age

Exclusion Criteria

* Weight below iso-BMI 30, according to the IOTF iso-BMI cut-off points
* Mental illness in the child or the parents that complicates attendance at activities.
* Physical limitations or illness that prevent the child from performing exercise
* If participant is not able to perform all 12 weeks of exercise for other reasons.
Minimum Eligible Age

8 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Regionshospital Nordjylland

OTHER_GOV

Sponsor Role lead

Responsible Party

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Tine Caroc Warner

Principal investigator, M.D.

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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RHN_TCW_01

Identifier Type: -

Identifier Source: org_study_id

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